Trials / Active Not Recruiting
Active Not RecruitingNCT05233527
Novosyn® Quick in Patients Undergoing Episiotomy Closure
Observational, Retrospective, Monocentric Clinical Study on the Safety of Novosyn® Quick in Women With a Spontaneous Vaginal Delivery Who Required an Indicated Episiotomy
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 229 (actual)
- Sponsor
- Aesculap AG · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Retrospective, monocentric clinical study on the clinical performance of Novosyn® Quick in patients undergoing episiotomy closure.
Detailed description
The study design is a retrospective, consecutive series of women with a spontaneous vaginal delivery who required an indicated episiotomy with Novosyn® Quick between the period January 2020 - December 2020 at Hospital General de Catalunya. All women treated with Novosyn® Quick between January 2020 - December 2020 at the Hospital General de Catalunya will be analyzed. The investigator team will access medical records for the cohort of patients identified.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Episiotomy Closure | indicated episiotomy with Novosyn® Quick after spontaneous vaginal delivery |
Timeline
- Start date
- 2024-05-09
- Primary completion
- 2026-03-26
- Completion
- 2026-10-01
- First posted
- 2022-02-10
- Last updated
- 2026-04-17
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT05233527. Inclusion in this directory is not an endorsement.